Examples of 'hydroxylamine hydrochloride' in a sentence
Meaning of "hydroxylamine hydrochloride"
hydroxylamine hydrochloride: Hydroxylamine hydrochloride is an inorganic compound with the chemical formula NH2OH·HCl. It is commonly used in various chemical reactions, such as in the synthesis of pharmaceuticals, organic compounds, and as a reducing agent. This compound can serve as a reagent in different chemical processes due to its properties and reactions
How to use "hydroxylamine hydrochloride" in a sentence
Basic
Advanced
hydroxylamine hydrochloride
Hydroxylamine halide such as hydroxylamine hydrochloride.
Hydroxylamine hydrochloride is generally preferred.
Free formaldehyde was determined by reaction with hydroxylamine hydrochloride.
Use of hydroxylamine hydrochloride to remove unwanted colour from hydrochloric acid.
The solution was filtered to remove unused hydroxylamine hydrochloride.
It is preferred to use hydroxylamine hydrochloride ( hydroxyl ammonium chloride ).
All solvents were removed under vacuum to give hydroxylamine hydrochloride.
Is treated with hydroxylamine hydrochloride to provide the oxime 2.
Usable electrolytes include dimethylamine hydrochloride and hydroxylamine hydrochloride.
Reacting the above product with hydroxylamine hydrochloride in an aqueous organic solvent.
Hydroxypyrimidine xvi is prepared from xv by treatment of the nitrile with hydroxylamine hydrochloride.
It was added 3 mmol hydroxylamine hydrochloride per litre hydrochloric acid.
The resulting protected sulfhydryl groups were exposed by reaction of the proteins with hydroxylamine hydrochloride.
The condensation of a ketone with hydroxylamine hydrochloride gives an oxime.
Hydroxylamine hydrochloride is corrosive, causes bums to any área of contact.
See also
In one embodiment, the deprotecting agent is hydroxylamine hydrochloride.
Alternatively, hydroxylamine hydrochloride is reacted with sodium acetate in a suitable solvent such as ethanol.
A method according to claim 1, wherein benzaldehyde is reacted with hydroxylamine hydrochloride.
The trichloromethyl -? - diketones react with hydroxylamine hydrochloride leading to three sets of isoxazole derivatives.
Hydroxylamine is preferably generated in situ from a hydroxylamine salt, such as hydroxylamine hydrochloride.
Compound 3 can be combined with hydroxylamine hydrochloride under suitable oxime formation conditions to form compound 4.
In addition, an oxime may be formed by treating the aldehyde with hydroxylamine hydrochloride.
Oxime formation with hydroxylamine hydrochloride in pyridine gives compound A-4 in excellent yield.
Reaction of i ( step a ) with chloral hydrate in the presence of hydroxylamine hydrochloride yields isatin ii.
A solution of hydroxylamine hydrochloride was prepared at a concentration of 63 mg / ml.
Method according to claim 1, characterised in that hydroxylamine hydrochloride is used as reducing agent.
Examples of suitable conductivity agents include dimethylamine hydrochloride, diethylamine hydrochloride, lithium nitrate, and hydroxylamine hydrochloride.
Treatment of 1 with hydroxylamine hydrochloride in pyridine affords compound 2.
For example, the substituted methanone of structure 8 can be reacted with pyridine and hydroxylamine hydrochloride.
Ten milliliters of a 5 wt / v % hydroxylamine hydrochloride solution was added to this solution.
The procedure of Example 11 is again followed except that the hydroxylamine salt is hydroxylamine hydrochloride.
Condensation of compounds 10 with hydroxylamine hydrochloride in a mixture of dioxane and pyridine gives compounds 11.
The process of claim 12, wherein the deprotecting agent is hydroxylamine hydrochloride.
To this hydroxylamine hydrochloride ( 2 eq ) was added and the reaction monitored by LCMS.
After 2.5h, the additions of triethylamine and hydroxylamine hydrochloride were repeated.
Hydroxylamine hydrochloride and urea were from EM Science ( Gibbstown, NJ ).
The oximes 2 ' are formed by reaction of 2 with hydroxylamine hydrochloride in pyridine.
Equivalents of hydroxylamine hydrochloride are added to a solution of para-hydroxyacetophenone in pyridine ( 16 % dilution ).
The 2,5-dimethylpyrrolyl protecting group is removed by reaction with hydroxylamine hydrochloride.
Compound ( II ) is reacted with hydroxylamine hydrochloride in pyridine to obtain compound ( III ).
Removal of the 2,5-dimethylpyrrolyl protecting group can be accomplished by reaction with hydroxylamine hydrochloride.
Microwave irradiation of phthalic anhydride and hydroxylamine hydrochloride in pyridine produces N-hydroxyphthalimide in 81 % yield.
The corresponding aldoxime is prepared by reacting the corresponding aldehyde with hydroxylamine hydrochloride at pH 9-10.
In the case of Example 5, N-methyl-hydroxylamine hydrochloride was substituted for hydroxylamine hydrochloride.
The method of claim 11, wherein the second reducing agent is hydroxylamine or hydroxylamine hydrochloride.
In Scheme A, a solution of hydroxylamine hydrochloride in water is chilled to 0°C.
A process according to claim 12, wherein the reaction of step b2 is carried out with hydroxylamine hydrochloride.
After stirring evenly, 17.3g hydroxylamine hydrochloride was slowly added in.
The procedure is as in Example 38, with the replacement of O-methylhydroxylamine with hydroxylamine hydrochloride.
Parts of this hydrochloride and 3.5 parts of hydroxylamine hydrochloride were stirred in 25 parts of water.
You'll also be interested in:
Examples of using Hydrochloride
Show more
Metformin hydrochloride is excreted unchanged in the urine
Precipitation of the imidazole hydrochloride started immediately
Ambroxol hydrochloride is secreted into breast milk
Examples of using Hydroxylamine
Show more
Hydroxylamine sulfate combined with hydrazine hydrate
Nitrile reacts with hydroxylamine to form amidoximes
Hydroxylamine ion was selectively adsorbed on the resin
